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Author Details

Yijun Huang
University of Wisconsin, Wisconsin EyeKor Inc.
1997
16
14
PMIDPaper TitleJournal TitlePublished Year
32679202Quantification of Geographic Atrophy Using Spectral Domain OCT in Age-Related Macular Degeneration.Ophthalmol Retina2021
27128499Variability in Spectral-Domain Optical Coherence Tomography over 4 Weeks by Age.Ophthalmic Epidemiol2016
25556116The epidemiology of vitreoretinal interface abnormalities as detected by spectral-domain optical coherence tomography: the beaver dam eye study.Ophthalmology2015
25461295Retinal thickness measured by spectral-domain optical coherence tomography in eyes without retinal abnormalities: the Beaver Dam Eye Study.Am J Ophthalmol2015
23761091Effect of optical coherence tomography scan decentration on macular center subfield thickness measurements.Invest Ophthalmol Vis Sci2013
24386127Development of a semi-automatic segmentation method for retinal OCT images tested in patients with diabetic macular edema.PLoS One2013
22427567Signal quality assessment of retinal optical coherence tomography images.Invest Ophthalmol Vis Sci2012
10634630Psychophysical evidence for rod vulnerability in age-related macular degeneration.Invest Ophthalmol Vis Sci2000
10655151Optical coherence tomography (OCT) abnormalities in rhodopsin mutant transgenic swine with retinal degeneration.Exp Eye Res2000
10440267Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degeneration.Invest Ophthalmol Vis Sci1999
10449795Stable transgene expression in rod photoreceptors after recombinant adeno-associated virus-mediated gene transfer to monkey retina.Proc Natl Acad Sci U S A1999
9804149Relation of optical coherence tomography to microanatomy in normal and rd chickens.Invest Ophthalmol Vis Sci1998
9804150Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) gene.Invest Ophthalmol Vis Sci1998
9618546Disease sequence from mutant rhodopsin allele to rod and cone photoreceptor degeneration in man.Proc Natl Acad Sci U S A1998
9331262Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR gene.Invest Ophthalmol Vis Sci1997
9286267Rod plateaux during dark adaptation in Sorsby's fundus dystrophy and vitamin A deficiency.Invest Ophthalmol Vis Sci1997
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Collaborators

Scheie Eye Institute, Perelman School of Medicine, University of Pennsylvania
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Co-authored papers 9
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Heersink School of Medicine, University of Alabama at Birmingham
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University of Alabama at Birmingham
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National Eye Institute, National Institutes of Health
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Kaiser Permanente San Francisco Medical Center
Co-authored papers 1
the Center for Genetics and Health Policy, Vanderbilt University Medical School
Co-authored papers 1
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b MacuLogix Inc.
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Johns Hopkins University School of Medicine
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